16-nor Limonoids from Harrisonia perforata as promising selective 11β-HSD1 inhibitors

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作者
Xiao-Hui Yan
Ping Yi
Pei Cao
Shi-Ying Yang
Xin Fang
Yu Zhang
Ying Bin Wu
Ying-Tong Leng
Yang Di
Xiao-Jiang Lv
机构
[1] State Key Laboratory of Phytochemistry and Plant Resources in West China,
[2] Kunming Institute of Botany,undefined
[3] Chinese Academy of Sciences,undefined
[4] College of Forestry,undefined
[5] Southwest Forestry University/Key Laboratory of Forest Disaster Warning and Control of Yunnan Province,undefined
[6] Key Laboratory of Chemistry for Natural Products of Guizhou Province and Chinese Academy of Sciences,undefined
[7] Beijing Key Laboratory of Polymorphic Drugs,undefined
[8] Institute of Materia Medica,undefined
[9] Chinese Academy of Medical Sciences & Peking Union Medical College,undefined
[10] Shanghai Institute of Materia Medica,undefined
[11] Chinese Academy of Sciences,undefined
来源
Scientific Reports | / 6卷
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摘要
Two new 16-nor limonoids, harperspinoids A and B (1 and 2), with a unique 7/5/5/6/5 ring system, have been isolated from the plant Harrisonia perforate together with a known one, Harperforin G (3). Their structures were elucidated by NMR spectroscopy, X-ray diffraction analysis and computational modelling. Compound 1 exists as polymorphic crystals. Conformations of 1 in solution were further discussed based on the computational results. These compounds exhibited notable inhibitory activity against the 11β-HSD1 enzyme. Compound 3 had potencies for the inhibition of human 11β-HSD1 with high selectivity against 11β-HSD2 (IC50 0.58 μM, SI > 174). Molecular docking and quantitative structure-activity relationship studies revealed a mixed regulatory mechanism.
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